Long-term tolerance after allergen immunotherapy is accompanied by selective persistence of blocking antibodies - 10/08/11
Abstract |
Background |
Grass pollen immunotherapy for allergic rhinitis is a disease-modifying treatment that results in long-term clinical tolerance lasting years after treatment discontinuation. Active treatment is associated with generation of inhibitory grass pollen–specific IgG antibodies capable of blocking allergen-IgE interactions.
Objectives |
We sought to investigate the involvement of IgG-associated inhibitory antibodies with long-term clinical tolerance after discontinuation of grass pollen immunotherapy.
Methods |
We conducted a 4-year study in which patients who had moderate-to-severe allergic rhinitis underwent a randomized, double-blind, placebo-controlled discontinuation of subcutaneous grass pollen immunotherapy. All subjects received grass pollen immunotherapy injections for 2 years (n = 13), followed by a further 2 years of either active (n = 7) or placebo (n = 6) injections. Clinical outcomes included seasonal symptoms and use of rescue medication. Serum specimens were collected at baseline and after 2 and 4 years for quantification of allergen-specific IgG antibodies. Sera were also tested for IgG-dependent inhibitory bioactivity against IgE-allergen binding in cellular assays by using flow cytometry and confocal microscopy to detect binding of IgE–grass pollen allergen complexes to B cells.
Results |
Clinical improvement was maintained after 2 years of discontinuation. Although immunotherapy-induced grass pollen–specific IgG1 and IgG4 levels decreased to near-preimmunotherapy levels during discontinuation, inhibitory bioactivity of allergen-specific IgG antibodies was maintained unchanged.
Conclusion |
Grass pollen immunotherapy induces a subpopulation of allergen-specific IgG antibodies with potent inhibitory activity against IgE that persists after treatment discontinuation and that could account for long-term clinical tolerance.
Le texte complet de cet article est disponible en PDF.Key words : Immunotherapy, IgE, IgG4, facilitated antigen presentation, CD23
Abbreviations used : FAB, IQR
Plan
Supported by grants from the Immune Tolerance Network (S.R.D.), Asthma UK (S.R.D. and S.J.T.), the Health Foundation (S.J.T.), and the London Law Trust (L.K.J.), and a Biotechnology and Biological Sciences Research Council (BBSRC) studentship case award (M.H.S.). |
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Disclosure of potential conflict of interest: S. M. Walker has received consulting fees and research support from ALK-Abelló. S. R. Durham has received lecture fees and research support from ALK-Abelló and has consulted for ALK-Abelló, Circassia, and Greer Laboratories. The rest of the authors have declared that they have no conflict of interest. |
Vol 127 - N° 2
P. 509 - février 2011 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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